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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
16 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1B
Papillary or follicular thyroid carcinoma

LMNA CCDC6
DIRC3
ERC1
FOXE1
GOLGA5
NCOA4
NDUFA13
NKX2-1
NTRK1
PCM1
RET
TFG
TPR
TRIM24
TRIM27
TRIM33


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.49)
TPR



Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1B
LMNA
Papillary or follicular thyroid carcinoma
CCDC6 DIRC3 ERC1 FOXE1 GOLGA5 NCOA4
NDUFA13 NKX2-1 NTRK1 PCM1 RET TFG
TPR TRIM24 TRIM27 TRIM33



Autosomal dominant limb-girdle muscular dystrophy type 1B
Papillary or follicular thyroid carcinoma

Synonym(s):
- LGMD1B
- Limb-girdle muscular dystrophy due to lamin A/C deficiency

Synonym(s):
- Well-differentiated thyroid carcinoma

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.